Genesⓘ

Dataset:
?Protein-coding genes with reviewed gene-disease associations only.
?Curated and unreviewed gene-disease associations.
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3381 to 3390 of 15448 Genes
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Entrez ID Gene Symbol Gene Name Synonyms Diseases

3381
Dendrocyte expressed seven transmembrane protein
FIND, TM7SF4, hDC-STAMP
Amphetamine or sympathomimetic abuse, Endometriosis, Diabetes mellitus type 2

3382
Dopachrome tautomerase
OCA8, TRP-2, TYRP2
Age-related macular degeneration, Oculocutaneous albinism, Pelvic organ prolapse, Scoliosis

3383
DCMP deaminase
-
Ankylosing spondylitis, Autoimmune disease, Autoimmune thyroid disease, Celiac disease, Central nervous system cancer, Common variable immunodeficiency, Crohn disease, Glioblastoma, Glioma, Granulomatosis with polyangiitis, Juvenile idiopathic arthritis, Neurotic disorder, Obesity, Psoriasis, Systemic lupus erythematosus
View all (2 more)

3384
Dynactin subunit 1
DAP-150, DP-150, HMND14, P135
Amyotrophic lateral sclerosis, Charcot-marie-tooth disease, Distal hereditary motor neuropathy, Distal spinal muscular atrophy, Frontotemporal dementia, Hereditary motor and sensory neuropathies, Motor neuron disease, Mood disorder, Parkinson disease, Peripheral neuropathy

3385
Dynactin subunit 2
DCTN50, DYNAMITIN, HEL-S-77, RBP50
Charcot-marie-tooth disease, Insomnia

3386
Dynactin subunit 3
DCTN-22, DCTN22
Bullous pemphigoid

3387
Dynactin subunit 4
DYN4, P62
Cholangiocarcinoma, Cystic fibrosis, Facial nerve disorder, Lung cancer

3388
Dynactin subunit 5
-
Bipolar disorder, Fanconi anemia

3389
Defective in cullin neddylation 1 domain containing 1
DCNL1, DCUN1L1, RP42, SCCRO, SCRO, Tes3
Parkinson disease

3390
Defective in cullin neddylation 1 domain containing 2
C13orf17, DCNL2
Epidermolysis bullosa, Ovarian epithelial cancer, Ovarian cancer